Understanding and Enhancing Health-Related Social Needs (HRSN) Screening Among Community Oncology Practices
试验速览
- 阶段
- 不适用
- 状态
- Enrolling By Invitation
- 入组人数
- 144
- 试验地点
- 71
- 主要终点
- HRSN screening reach (Part 1)
研究概览
简要总结
This study evaluates health related social needs screening processes in community oncology clinics.
详细描述
The primary objective of this study is to assess current processes around health related social needs (HRSN) screening among NCORP clinics and categorize clinics based on their implementation of HRSN screening. The primary endpoint will be a detailed understanding of current processes, with attention to variability by key clinic characteristics.
There are 3 parts of the study in which participants can participate in one or all parts (3 total).
Part 1: Participants attend training, complete clinic assessments and observations and may complete an interview on study.
Part 2: Identified clinic staff will be interviewed to discuss factors that influence HRSN screening at their clinic and help develop generalized guidance.
Part 3: Participants attend a co-design workshop and complete surveys on study feasibility.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •NCORP PRACTICES:
- •Must be an affiliate or sub-affiliate of an NCORP Community or Minority Underserved Community site
- •Must provide outpatient oncology care
- •Must be a NCORP practice (defined as one or more NCORP affiliates/sub-affiliates, that have a common administrative structure and share providers and/or patients)
- •Must have identified two or more Practice Staff that are available and willing to participate on the Practice Interest Form
- •Must have identified at least 1-3 outpatient oncology clinics willing to participate on the Practice Interest Form
- •1-3 clinics within the practice should be selected
- •Clinics may or may not be located in different physical locations
- •The investigators will encourage NCORP practices to select clinics within a practice that differ in current or potential implementation of health related social needs (HRSN) screening (e.g., different clinic workflow or staff, different screening triggers, different tools), so that heterogeneity within NCORP practices can be captured
- •Clinics must be willing to allow Practice Staff participants to observe the clinical operations in-person
- •PRACTICE STAFF:
- •Must be willing and able to take time to observe in person and document 1-3 selected clinics within the practice (approximately 2-3 hours per clinic)
- •Must be staff at the selected and enrolled practice. Suggestions of appropriate staff are cancer care delivery research (CCDR) Lead, research nurse, clinical research coordinator or NCORP Administrators. Staff members with primary clinical roles may also be appropriate, if available
- •Must be willing and able to participate in two 1.5 hour virtual training sessions
- •Must be willing to interview Clinic Key Informants (approximately 30 minutes per interview; in-person or remotely over the internet or by phone)
- •If the clinic is chosen for Part 2, must be willing to schedule an interview between Clinic Key Informant and Wake Forest health HRSN Study Team or designee
- •If the clinic is chosen for Part 3, must be willing to participate in a three hour or two 1.5 hour in-person (if possible) workshop(s). If the clinic schedules an in-person workshop, there will be no hybrid or separate virtual option for those that cannot attend
- •Must be willing to be recorded when participating in interviews and the workshop.
- •CLINIC KEY INFORMANT:
- •Must be willing to participate in Part 1 Operational Assessment, which involves a semi-structured interview (approximately 30 minutes; in-person or remotely over the internet or by phone) and a brief Non-patient Demographics Survey (approximately 5 minutes)
- •If the clinic is chosen for Part 2, must be willing to participate in an additional 45 minute interview (remotely over the internet or by phone)
- •If the clinic is chosen for Part 3, must be willing to participate in a three hour or two 1.5 hour in-person (if possible) workshop(s). If the clinic schedules an in-person workshop, there will be no hybrid or separate virtual option for those that cannot attend
- •STAFF WORKSHOP PARTICIPANT:
- •Must be a clinic stakeholder (e.g., providers, practice managers, etc.) of the selected clinic
- •Must be willing and able to participate in a three hour or two 1.5 hour in-person (if possible) recorded workshop. If the clinic schedules an in-person workshop, there will be no hybrid or separate virtual option for those that cannot attend
- •Must be willing to be recorded when participating in interviews and the workshop.
- •PATIENT WORKSHOP PARTICIPANT:
- •Must be a prospective clinic stakeholder (e.g., patient representative) of the selected clinic
- •Must be willing and able to participate in a three hour or two 1.5 hour in-person (if possible) recorded workshop. If the clinic schedules an in-person workshop, there will be no hybrid or separate virtual option for those that cannot attend
- •Must have received cancer treatment at the selected clinic within the last five years
- •Must be willing to be recorded when participating in the workshop.
排除标准
- •PRACTICE STAFF:
- •** Unable to understand, read and communicate in English, as the trainings and observations will be documented in English
- •STAFF WORKSHOP PARTICIPANT:
- •** Unable to understand, read and communicate in English, as the workshop will be conducted in English
- •PATIENT WORKSHOP PARTICIPANT:
- •** Unable to understand, read and communicate in English, as the workshop will be conducted in English
研究组 & 干预措施
Part 1
Part 1: Participants attend training, complete clinic assessments and observations and may complete an interview on study.
干预措施: Non-Interventional (Other)
Part 2
Part 2: Identified clinic staff will be interviewed to discuss factors that influence health related social needs (HRSN) screening at their clinic and help develop generalized guidance.
干预措施: Non-Interventional (Other)
Part 3
Part 3: Participants attend a co-design workshop and complete surveys on study feasibility.
干预措施: Non-Interventional (Other)
结局指标
主要结局
HRSN screening reach (Part 1)
时间窗: From study enrollment to approximately 4 and 16 weeks post initial study training
Determining the perception of the proportion of patients at clinics who are screened for health related social needs (HRSN).
Generation of a tailored implementation plan for each participating clinic
时间窗: Between time of clinic selection and co-design workshop completion, to be no more than 6 months
Generation (defined for each clinic as completed or not completed) of a tailored implementation plan for each participating clinic in Part 3 that includes (1) adaptations to current HRSN screening and follow-up processes, and (2) potential implementation strategies to enhance HRSN screening implementation.
Barriers and facilitators influencing HRSN screening implementation
时间窗: From study enrollment to time completion of key informant interviews, approximately within 6 months
Synthesize themes to create a list of barriers and facilitators influencing HRSN screening implementation within high-implementation clinics, moderate-implementation clinics, and low-implementation clinics.
次要结局
未报告次要终点